Schwan W R, Demuth A, Kuhn M, Goebel W
Lehrstuhl für Mikrobiologie, Theodor-Boveri-Institut für Biowissenschaften, Universität Würzburg, Germany.
Infect Immun. 1994 Nov;62(11):4795-803. doi: 10.1128/iai.62.11.4795-4803.1994.
Listeria monocytogenes is a facultative intracellular organism that is capable of replicating within macrophage and macrophage-like cells. The species secretes a phosphatidylinositol-specific phospholipase C (PI-PLC) encoded by the plcA gene. A plcA gene from L. monocytogenes was cloned downstream of a gram-positive promoter in the plasmid pWS2-2. To determine what effect plcA would have on intracellular survival when introduced into Listeria innocua, a species that does not growth intracellularly or contain plcA, transformation with the recombinant pWS2-2 plasmid was performed. Phospholipase C activity in Listeria innocua/pWS2-2 was confirmed on a brain heart infusion-phosphatidylinositol agar plate, whereas wild-type L. innocua did not produce PI-PLC activity. Intracellular growth of L. innocua/pWS2-2 was subsequently measured in the macrophage-like cell line J774 by Giemsa staining and viable count determinations at specific time points following infection. The J774 cells infected with wild-type L. innocua showed a falling viable count through 8 h postinfection. Although J774 cells infected with L. innocua/pWS2-2 also initially displayed reduced viable counts, the viable count rose after 6 h postinfection and increased further at 8 h postinfection before a subsequent decline again at 16 h postinfection. Giemsa staining revealed fewer than 6 bacteria in individual macrophage cells at 2 h postinfection, and yet approximately 15% of the J774 cells had 6 to 12 bacteria localized to one area of the macrophage cell after 6 h; moreover, electron micrographs showed that the L. innocua/pWS2-2 cells were replicating inside the phagosome of the host cell. Furthermore, Thoria Sol labeling demonstrated that lysosomes had fused with these phagosomes, and acridine orange staining revealed that the compartments were acidified. These results demonstrate that L. innocua cells transformed with the plasmid-borne plcA gene, and expressing functional PI-PLC, are able to grow intracellularly in what appear to be phagolysosomes, although between 3 and 6 h is needed for this to manifest itself. Intracellular growth specifically in L. innocua may be a secondary function associated with the plcA gene product. The addition of this one gene, plcA, to a species of Listeria that in the wild-type state does not replicate intracellularly apparently can now allow some of the bacteria to transiently multiply inside the phagosomes of host macrophage cells.
单核细胞增生李斯特菌是一种兼性胞内菌,能够在巨噬细胞和类巨噬细胞内复制。该菌种分泌一种由plcA基因编码的磷脂酰肌醇特异性磷脂酶C(PI-PLC)。将来自单核细胞增生李斯特菌的plcA基因克隆到质粒pWS2-2中革兰氏阳性启动子的下游。为了确定将plcA导入无害李斯特菌(一种不在细胞内生长且不含plcA的菌种)时对其细胞内存活有何影响,进行了重组pWS2-2质粒的转化。在脑心浸液-磷脂酰肌醇琼脂平板上证实了无害李斯特菌/pWS2-2中的磷脂酶C活性,而野生型无害李斯特菌不产生PI-PLC活性。随后通过吉姆萨染色和在感染后特定时间点进行活菌计数,在类巨噬细胞系J774中测量了无害李斯特菌/pWS2-2的细胞内生长情况。感染野生型无害李斯特菌的J774细胞在感染后8小时内活菌数下降。虽然感染无害李斯特菌/pWS2-2的J774细胞最初活菌数也减少,但在感染后6小时活菌数上升,在感染后8小时进一步增加,随后在感染后16小时再次下降。吉姆萨染色显示在感染后2小时单个巨噬细胞内细菌少于6个,但在6小时后约15%的J774细胞有6至12个细菌聚集在巨噬细胞的一个区域;此外,电子显微镜照片显示无害李斯特菌/pWS2-2细胞在宿主细胞的吞噬体内复制。此外,钍溶胶标记表明溶酶体已与这些吞噬体融合,吖啶橙染色显示这些区室已酸化。这些结果表明,用携带plcA基因的质粒转化并表达功能性PI-PLC的无害李斯特菌细胞能够在似乎是吞噬溶酶体的细胞内生长,尽管这需要3至6小时才能显现出来。无害李斯特菌中的细胞内生长可能是与plcA基因产物相关的次要功能。将这个单一基因plcA添加到野生型状态下不在细胞内复制的李斯特菌种中,显然现在可以使一些细菌在宿主巨噬细胞的吞噬体内短暂繁殖。